HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 886749Generated: October 26, 2026
Tetrahydrofuran → 4-Chloro-2-(methylsulfonyl)thieno[2,3-d]pyrimidine
https://huagongshe.com/reaction/886749
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Chloro-2-(methylthio)thieno[2,3-d]pyrimidine | HCID 21988351 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Chloro-2-(methylsulfonyl)thieno[2,3-d]pyrimidine | HCID 21988354 | — |
Reaction Steps
To 1 L round-bottom flask was added 4-chloro-2-(methylthio)thieno[2,3-d]pyrimidine (35.0 g, 162 mmol), THF (300 mL). The solution was stirred at 0° C. and treated dropwise with a solution of OXONE (209 g, 339 mmol) in water (350 mL). The resulting mixture was stirred at RT overnight. The reaction mixture was diluted with EtOAc (500 mL) and water (300 mL). Separated the layers, the aqueous layer was extracted with EtOAc (3×300 mL). Organic layers were combined, washed with brine (2×300 mL), dried over MgSO4, filtered and concentrated to give (33 g). MS (ES+): 249 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08247409B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-823dfb502cc941848f95bd7066106d79 |
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| Source note | uspto-grants-2012_08 |
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